A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116214



Internal ID21463454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37606511..37606511hg38UCSC Ensembl
chr20:36234913..36234913hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382427
hg192427
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665270
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116214
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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